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Nabumetone

NDC 80425-0053 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078671
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNABUMETONE (500 mg/1)
Marketing started20190306
Package count1

External sources

Source: openFDA. Public-domain (CC0).